Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
40301 BAA01g25580 A01 13919668 C T upstream_gene_variant MODIFIER c.-3734G>A| S18
40302 BAA01g25580 A01 13920630 C T upstream_gene_variant MODIFIER c.-4696G>A| S231
40303 BAA01g25590 A01 13920771 C T missense_variant MODERATE c.1340C>T|p.Pro447Leu S111
40304 BAA01g25590 A01 13921060 G A intron_variant MODIFIER c.1502-27G>A| S308
40305 BAA01g25590 A01 13921655 C T downstream_gene_variant MODIFIER c.*234C>T| S36
40306 BAA01g25590 A01 13921790 G A downstream_gene_variant MODIFIER c.*369G>A| S60
40307 BAA01g25600 A01 13922880 C T upstream_gene_variant MODIFIER c.-4966C>T| S282
40308 BAA01g25600 A01 13923155 C T upstream_gene_variant MODIFIER c.-4691C>T| S305
40309 BAA01g25600 A01 13924171 C T upstream_gene_variant MODIFIER c.-3675C>T| S264
40310 BAA01g25600 A01 13925487 C T upstream_gene_variant MODIFIER c.-2359C>T| S112
40311 BAA01g25600 A01 13925777 G A upstream_gene_variant MODIFIER c.-2069G>A| S132
S89
40312 BAA01g25600 A01 13926845 G A upstream_gene_variant MODIFIER c.-1001G>A| S294
40313 BAA01g25600 A01 13926976 G A upstream_gene_variant MODIFIER c.-870G>A| S294
40314 BAA01g25600 A01 13927112 C T upstream_gene_variant MODIFIER c.-734C>T| S136
40315 BAA01g25600 A01 13928067 C T synonymous_variant LOW c.222C>T|p.Ser74Ser S255
40316 BAA01g25600 A01 13928556 G A synonymous_variant LOW c.711G>A|p.Pro237Pro S15
S2
S3
S34
S4
S6
40317 BAA01g25610 A01 13929813 C T missense_variant MODERATE c.1664G>A|p.Arg555Lys S184
40318 BAA01g25600 A01 13930470 C T downstream_gene_variant MODIFIER c.*1419C>T| S295
40319 BAA01g25600 A01 13930800 C T downstream_gene_variant MODIFIER c.*1749C>T| S159
S243
40320 BAA01g25600 A01 13931112 C T downstream_gene_variant MODIFIER c.*2061C>T| S67
40321 BAA01g25610 A01 13931187 C T missense_variant MODERATE c.970G>A|p.Glu324Lys S87
40322 BAA01g25600 A01 13931555 G A downstream_gene_variant MODIFIER c.*2504G>A| S268
40323 BAA01g25610 A01 13931633 G A missense_variant MODERATE c.893C>T|p.Pro298Leu S37
40324 BAA01g25600 A01 13932174 C T downstream_gene_variant MODIFIER c.*3123C>T| S177
40325 BAA01g25610 A01 13932439 C A missense_variant MODERATE c.551G>T|p.Gly184Val S133